Anti-inflammatory effects of hepatocyte growth factor: induction of interleukin-1 receptor antagonist

Hepatocyte growth factor (HGF) prevents liver failure in various animal models including endotoxin-induced acute liver failure. We were interested to find out whether human HGF exerts anti-inflammatory effects by modulation of cytokine synthesis. Therefore, human HepG2 cells were cultured with increasing concentrations of HGF. HGF dose-dependently upregulated the production of interleukin-1 receptor antagonist (IL-1Ra). Incubation of HepG2 cells with interleukin-1beta (IL-1beta) caused an increase in IL-1Ra levels, while interleukin-6 (IL-6) had no effect on IL-1Ra synthesis. Co-stimulation of HepG2 cells with HGF + IL-1beta resulted in a synergistic effect on IL-1Ra mRNA and protein expression. Stimulation of freshly isolated mouse hepatocytes from male C57 BL/6 mice with HGF increased IL-1Ra mRNA and protein synthesis dose-dependently. A co-stimulation with HGF and IL-1beta had a synergistic effect on IL-1Ra mRNA expression but only a partially additive effect on IL-1Ra protein synthesis. HGF-induced IL-1Ra production was significantly decreased by the mitogen-activated protein kinase (MAPK) inhibitor PD98059. Accordingly, HGF stimulation specifically increased MAPK-dependent signalling pathway (p42/44). In contrast, in preactivated PBMC mRNA expression and protein synthesis of IL-1Ra, interleukin-10 (IL-10) and tumor necrosis factor-alpha (TNF-alpha) were unaffected after stimulation with HGF. In conclusion, our data suggest that HGF exerts anti-inflammatory effects by modulating the signal transduction cascade leading to increased expression of IL-1Ra, which might explain the protective and regenerative properties of this cytokine in animal models of liver failure.     

Modulation of cardiac PIP2 by cardioactive hormones and other physiologically relevant interventions

Phosphatidylinositol4,5-bisphosphate (PIP₂) affects profoundly several cardiacion channels and transporters, and studies ofPIP₂-sensitive currents in excised patches suggest thatPIP₂ can be synthesized and broken down within 30 s.To test when, and if, total phosphatidylinositol 4-phosphate (PIP) andPIP₂ levels actually change in intact heart, we used a new,nonradioactive HPLC method to quantify anionic phospholipids. Total PIPand PIP₂ levels (10-30 µmol/kg wet weight) do notchange, or even increase, with activation ofG_q/phospholipase C (PLC)-dependent pathways by carbachol(50 µM), phenylephrine (50 µM), and endothelin-1 (0.3 µM).Adenosine (0.2 mM) and phorbol 12-myristate 13-acetate (1µM) bothcause 30% reduction of PIP₂ in ventricles, suggesting thatdiacylglycerol (DAG)-dependent mechanisms negatively regulate cardiacPIP₂. PIP₂, but not PIP, increases reversiblyby 30% during electrical stimulation (2 Hz for 5 min) in guinea pigleft atria; the increase is blocked by nickel (2 mM). Both PIP andPIP₂ increase within 3 min in hypertonic solutions, roughlyin proportion to osmolarity, and similar effects occur in multiple celllines. Inhibitors of several volume-sensitive signaling mechanisms do not affect these responses, suggesting that PIP₂ metabolismmight be sensitive to membrane tension, per se.

     

A mechanistic investigation on the formation and rearrangement of silaspiropentane: A theoretical study

The formation of silaspiropentane from addition of singlet silacyclopropylidene 1 and silacyclopropylidenoid 8 to ethylene has been investigated separately at the B3LYP, X3LYP, WB97XD, and M05–2X theories using the 6–31+G(d,p) basis set. The silacycloproylidenoid addition follows a stepwise route. In contrast, a concerted mechanism occurs for silacyclopropylidene addition. Moreover, the intramolecular rearrangements of silaspiropentane 9 to methylenesilacyclobutane 11 and 2-silaallene?+?ethylene 12 have been studied extensively. The required energy barrier for the isomerization of 9 to 10 was determined to be 44.0 kcal mol^?1 at the B3LYP/6–31+G(d,p) level. After formation of 10, the rearrangement to methylenesilacyclobutane 12 is highly exergonic by ?15.9 kcal mol^?1, which makes this reaction promising. However, the conversion of 9 to 11 is calculated to be quite endergonic, by 26.5 kcal mol^?1.     

Synthesis of mono Mannich bases of 2-(4-hydroxybenzylidene)-2,3-dihydroinden-1-one and evaluation of their cytotoxicities

Chalcones and Mannich bases are a group of compounds known for their cytotoxicities. In this study restricted chalcone analogue, compound 2-(4-hydroxybenzylidene)-2,3-dihydroinden-1-one MT1, was used as a starting compound to synthesize new mono Mannich bases since Mannich bases may induce more cytotoxicity than chalcone analogue that they are derived from by producing additional alkylating center for cellular thiols. In this study, cyclic and acyclic amines were used to synthesize Mannich bases. All compounds were tested against Ca9–22 (gingival carcinoma), HSC-2, HSC-3 and HSC-4 (oral squamous cell carcinoma) as tumour cell lines and HGF (gingival fibroblasts), HPC (pulp cells) and HPLF (periodontal ligament fibroblasts) human normal oral cells as non tumour cell lines. Cytotoxicity, selectivity index (SI) values and potency selectivity expression (PSE) values expressed as a percentage were determined for the compounds. According to data obtained, the compound MT8 with the highest PSE value bearing N-methylpiperazine moiety seems to be a good candidate to develop new cytotoxic compounds and is suited for further investigation.     

Carbonic anhydrase inhibition and cytotoxicity studies of Mannich base derivatives of thymol

Mannich bases of thymol were synthesized. The aminomethylation reaction was realised in the ortho position of the phenol for compounds 2 (dipropylamine), 3 (benzylamine), and 4 (dibenzylamine) while it was from para position for 1 (dimethylamine), 5 (piperidine), 6 (morpholine) and 7 (N-methylpiperazine). The carbonic anhydrase (CA, EC 4.2.1.1) inhibitory effects of the compounds were asssessed against hCA I and hCA II. All compounds moderately inhibited hCA I and hCA II. The cytotoxicity of the compounds against four human oral squamous cell carcinoma cell lines were compared those against three normal oral cells. Tumor specificity values were about 2 or slightly more for the compounds 2, 3, 4, 5 and 6. Compound 2 showed cytostatic activity against OSCC cell lines at 16 to 32-fold lower concentrations as compared with normal cells. This suggests that compound 2 can be considered as cytotoxicity enhancing drug candidate for further investigations.     

β Cell-Specific Deletion of the IL-1 Receptor Antagonist Impairs β Cell Proliferation and Insulin Secretion

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Floral development in <Emphasis Type="Italic">Thermopsis turcica</Emphasis>, an unusual multicarpellate papilionoid legume

The vast majority of the species of family Leguminosae have an apocarpous monomerous gynoecium. However, only a few taxa regularly produce multicarpellate gynoecia. The only known species of papilionoid legumes which has both a typical “flag blossom” and more than one carpel is Thermopsis turcica (tribe Thermopsideae). We studied the floral ontogeny of T. turcica with special reference to its gynoecium initiation and development. Flowers arise in simple terminal racemes in a helical order and are subtended by bracts. Bracteoles are initiated but then suppressed. Sepals appear more or less simultaneously. Then, petals emerge and remain retarded in development until later stages. The gynoecium usually includes three carpels with an abaxial one initiating first and two adaxial carpels arising later and developing somewhat asynchronously. The abaxial carpel appears concomitant with the outer stamens and is always oriented with its cleft toward the adaxial side, while the adaxial carpels face each other with their clefts and have them slightly turned to the adaxial side. Rarely uni-, bi- or tetracarpellate flowers arise. Seed productivity of T. turcica is on approximately the same level as in unicarpellate species of Thermopsis hence supporting the fact that the multicarpellate habit is adaptive or at least not harmful in this species.